HomePrimary Cell CultureBovine Brain Artery Endothelial Cells (BBAEC) Culture Protocol

Bovine Brain Artery Endothelial Cells (BBAEC) Culture Protocol

I. Storage

A. Cryopreserved Vials (B800-05)

Store the cryovials in a liquid nitrogen storage tank immediately upon arrival.

*Be sure to wear face protection mask and gloves when retrieving cryovials from the liquid nitrogen storage tank. The dramatic temperature change from the tank to the room could cause any trapped liquid nitrogen in the cryovials to burst and cause injury.

II. Preparation for Culturing

  1. Ensure the Class II Biological Safety Cabinet, with HEPA filtered laminar airflow, is in proper working condition.
  2. Sterilize the Biological Safety Cabinet with 70% alcohol.
  3. Turn the Biological Safety Cabinet blower on for 10 minutes before beginning cell culture work.
  4. Make sure all serological pipettes, pipette tips and reagent solutions are sterile.
  5. Follow the standard sterilization technique and safety rules:
    a. Do not pipette by mouth.
    b. Always wear gloves and safety glasses when working with animal cells even though all the animals have
    been inspected by the USDA.
    c. Handle all cell culture work in a sterile hood.

III. Culturing BBAEC

A. Preparing Cell Culture Flask

  1. Swirl the Attachment Factor Solution (123-100) bottle a few times to form a homogenous solution.
  2. Decontaminate the bottle with 70% alcohol in a sterile hood.
  3. Coat T-75 flasks (SIAL0641) by adding 7.5 ml of Attachment Factor Solution (123-100)* and rock the flasks gently to distribute the solution evenly to cover the whole culture surface.
  4. Coat the culture ware for 30 minutes at 37 °C or for 2 hours to overnight at room temperature.
  5. Remove the Attachment Factor Solution (123-100) by aspiration in a sterile hood.
  6. The coated flask can be used immediately or stored at 4 °C for up to 2 weeks.
  7. Prepare the coated flask for culturing BBAEC by pipetting 15 ml of Bovine Brain Endothelial Growth Medium (B819-500)** into this coated T-75 flask and wait for seeding.
    *The coating concentration is 1 ml per 10 cm2 surface area of culture ware.
    - 2.5 ml for coating a T-25 flask (SIAL0639) or a 60 mm tissue culture dish (SIAL0166).
    - 7.5 ml for coating a T-75 flask (SIAL0641) or a 100 mm tissue culture dish (SIAL0167).
    **Keep the medium to surface area ratio at 1-1.5ml per 5 cm2.
    - 5 ml for a T-25 flask (SIAL0639) or a 60 mm tissue culture dish (SIAL0166).
    - 15 ml for a T-75 flask (SIAL0641) or a 100 mm tissue culture dish (SIAL0167).

B. Thawing and Plating BBAEC

  1. Remove the cryopreserved vial of BBAEC from the liquid nitrogen storage tank using proper protection for your eyes and hands.
  2. Turn the vial cap a quarter turn to release any liquid nitrogen that may be trapped in the threads, then re-tighten the cap.
  3. Thaw the cells quickly by placing the lower half of the vial in a 37 °C water bath and watch the vial closely during the thawing process.
  4. Remove the vial from the water bath when only a small amount of ice is left in the vial. Do not let cells thaw completely.
  5. Decontaminate the vial exterior with 70% alcohol in a sterile Biological Safety Cabinet.
  6. Remove the vial cap carefully. Do not touch the rim of the cap or the vial with your hands to avoid contamination.
  7. Resuspend the cells in the vial by gently pipetting the cells 5 times with a 2 ml pipette. Be careful not to pipette too vigorously as to cause foaming.
  8. Pipette the cell suspension (1ml) from the vial into the T-75 flask (SIAL0641) containing 15 ml of Bovine Brain Endothelial Growth Medium (B819-500).
  9. Cap the flask and rock gently to evenly distribute the cells.
  10. Place the T-75 flask (SIAL0641) in a 37 °C, 5% CO2 humidified incubator. Loosen the cap to allow gas exchange. For best results, do not disturb the culture for 24 hours after inoculation.
  11. Change to fresh Bovine Brain Endothelial Growth Medium (B819-500) after 24 hours or overnight to remove all traces of DMSO.
  12. Change Bovine Brain Endothelial Growth Medium (B819-500) every other day until the cells reach 60% confluency.
  13. Double the Bovine Brain Endothelial Growth Medium (B819-500) volume when the culture is >60% confluent or for weekend feedings.
  14. Subculture the cells when the BBAEC culture reaches 80% confluency.

IV. Subculturing BBAEC

A. Preparing Subculture Reagents

  1. Remove the Trypsin-EDTA solution (T3924) and Trypsin Inhibitor (T6414) from the -20 °C freezer and thaw overnight in a refrigerator.
  2. Make sure all the subculture reagents are thawed. Swirl each bottle gently several times to form homogeneous solutions.
  3. Store all the subculture reagents at 4 °C for future use.
  4. Aliquot Trypsin/EDTA solution (T3924) and store the unused portion at -20 °C if only a portion of the Trypsin/EDTA (T3924) is needed.

B. Preparing Culture Flask

Prepare as in Step III A.

C. Subculturing BBAEC

Trypsinize Cells at Room Temperature. Do Not Warm Any Reagents to 37 °C.

  1. Remove the medium from culture flasks by aspiration.
  2. Wash the monolayer of cells with HBSS (H6648) and remove the solution by aspiration.
  3. Pipette 5 ml of Trypsin/EDTA Solution (T3924) into the T-75 flask (SIAL0641). Rock the flask gently to ensure the solution covers all the cells.
  4. Remove 4.5 ml of the solution immediately.
  5. Re-cap the flask tightly and monitor the trypsinization progress at room temperature under an inverted microscope. It usually takes about 1 minute for the cells to become rounded.
  6. Release the rounded cells from the culture surface by hitting the side of the flask against your palm until most of the cells are detached.
  7. Pipette 5 ml of Trypsin Inhibitor Solution (T6414) to the flask to inhibit further tryptic activity.
  8. Transfer the cell suspension from the flask to a 50 ml sterile conical tube.
  9. Rinse the flask with an additional 5 ml of Trypsin Inhibitor Solution (T6414) and transfer the solution into the same conical tube.
  10. Examine the T-75 flask (SIAL0641) flask under a microscope. If there are >20% cells left in the flask, repeat Steps 2-9.
  11. Centrifuge the conical tube at 220 x g for 5 minutes to pellet the cells.
  12. Aspirate the supernatant from the tube without disturbing the cell pellet.
  13. Flick the tip of the conical tube with your finger to loosen the cell pellet.
  14. Resuspend the cells in 5 ml of Bovine Brain Endothelial Growth Medium (B819-500) by gently pipetting the cells to break up the clumps.
  15. Count the cells with a hemocytometer or cell counter. Inoculate at 7,500 cells per cm2 for rapid growth, or at 5,000 cells per cm2 for regular subculturing.
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